Actively Recruiting

Age: 18Years +
All Genders
NCT03407469

Measurement of Adherence and Health-Related Quality of Life, and Health-Care Resource Utilization

Led by M.D. Anderson Cancer Center · Updated on 2025-11-18

260

Participants Needed

4

Research Sites

467 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this research study is to learn about the quality of life, experiences with treatment, and healthcare costs of patients who are receiving long-term treatment for venous thromboembolism (VTE) that is related to cancer. This is an investigational study. Up to 260 participants will be enrolled in this multicenter study. Up to 170 will take part in MD Anderson.

CONDITIONS

Official Title

Measurement of Adherence and Health-Related Quality of Life, and Health-Care Resource Utilization

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult (≥ 18 years) female or male subjects
  • Confirmed symptomatic proximal or distal lower extremity deep venous thrombosis with or without pulmonary embolism or other venous thromboses
  • Cancer (other than basal-cell or squamous-cell carcinoma of the skin), either active or diagnosed within 2 years prior to VTE with histopathologic diagnosis
  • Intention for long-term treatment (at least 3 months) with anticoagulation
  • Enrollment within the first 5 days from initiation of anticoagulation
  • Able to provide informed consent and complete study survey tools
  • Able to read and speak English
Not Eligible

You will not qualify if you...

  • Indication for anticoagulation other than cancer-related VTE
  • Eastern Cooperative Oncology Group (ECOG) Performance Status of 4 at enrollment
  • Life expectancy less than 3 months
  • Isolated pulmonary embolism, isolated upper extremity deep venous thrombosis, isolated splanchnic venous thrombosis, or isolated cerebral venous thrombosis confirmed by imaging

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 4 locations

1

University of Texas MD Anderson Cancer Center

Houston, Texas, United States, 77030

Actively Recruiting

2

Fundacion Valle del Lili

Cali, Colombia

Actively Recruiting

3

Hospital Clinic

Barcelona, Carrer de Villarroel, 170, Spain, 08036

Actively Recruiting

4

Hospital German Trias i Pujol

Barcelona, Spain, 08916

Actively Recruiting

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Research Team

C

Cristhiam M. Rojas Hernandez, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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